FDA.reportPublic FDA data

NDC 75839-810

This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.

Requested NDC
75839-810
Product root
75839-810
Identity scope
Product
Primary current NDC product row
Not present

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Dataset, Scope, Package NDC table
DatasetScopePackage NDC
unfinished productproduct
unfinished packagepackage75839-810-05
unfinished packagepackage75839-810-11
unfinished packagepackage75839-810-02
unfinished packagepackage75839-810-10
unfinished packagepackage75839-810-00
unfinished packagepackage75839-810-01
unfinished packagepackage75839-810-25

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.